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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974588insertion1nstd209human GRCh38 chr11: 111,766,393-111,766,393 , GRCh37.p13 chr11|NW_003871080.1: 18,385-18,385 , GRCh37.p13 chr11: 111,637,117-111,637,117 PPP2R1B
    nsv5920856copy number variation1nstd209human GRCh38 chr11: 111,722,480-111,725,268 , GRCh37.p13 chr11: 111,593,204-111,595,992 SIK2, PPP2R1B
    nsv5915084copy number variation1nstd209human GRCh38 chr11: 111,692,162-111,693,142 , GRCh37.p13 chr11: 111,562,886-111,563,866 SIK2, PPP2R1B
    nsv5699377mobile element insertion1nstd211human GRCh38 chr11: 111,701,714-111,701,714 , GRCh37.p13 chr11: 111,572,438-111,572,438 PPP2R1B, SIK2
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5657822insertion1nstd207human GRCh38 chr11: 111,746,202-111,746,202 , GRCh37.p13 chr11: 111,616,926-111,616,926 PPP2R1B
    nsv5654456insertion1nstd207human GRCh38 chr11: 111,766,393-111,766,393 , GRCh37.p13 chr11|NW_003871080.1: 18,385-18,385 , GRCh37.p13 chr11: 111,637,117-111,637,117 PPP2R1B
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5508118copy number variation1nstd206human GRCh38 chr11: 111,692,192-111,693,120 , GRCh37.p13 chr11: 111,562,916-111,563,844 PPP2R1B, SIK2
    nsv5421635mobile element insertion1nstd206human GRCh38 chr11: 111,701,714-111,701,765 , GRCh37.p13 chr11: 111,572,438-111,572,489 SIK2, PPP2R1B
    nsv5418207mobile element insertion1nstd206human GRCh38 chr11: 111,756,349-111,756,400 , GRCh37.p13 chr11|NW_003871080.1: 8,341-8,392 PPP2R1B
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5348290translocation1nstd200human GRCh38 chr11: 111,690,656-111,690,656 , GRCh38 chr11: 111,690,379-111,690,379 , GRCh37.p13 chr11: 111,561,380-111,561,380 , GRCh37.p13 chr11: 111,561,103-111,561,103 SIK2, PPP2R1B
    nsv5271482copy number variation1nstd204human GRCh38.p13 chr11: 111,690,845-111,693,200 , GRCh37.p13 chr11: 111,561,569-111,563,924 PPP2R1B, SIK2
    nsv5199906mobile element insertion1nstd203human GRCh38 chr11: 111,746,209-111,746,218 , GRCh37.p13 chr11: 111,616,933-111,616,942 PPP2R1B
    nsv5196711mobile element insertion1nstd203human GRCh38 chr11: 111,746,208-111,746,218 , GRCh37.p13 chr11: 111,616,932-111,616,942 PPP2R1B
    nsv5193300mobile element insertion1nstd203human GRCh38 chr11: 111,746,205-111,746,218 , GRCh37.p13 chr11: 111,616,929-111,616,942 PPP2R1B
    nsv5182861mobile element insertion1nstd203human GRCh38 chr11: 111,746,202-111,746,218 , GRCh37.p13 chr11: 111,616,926-111,616,942 PPP2R1B
    nsv5129276mobile element insertion1nstd203human GRCh38 chr11: 111,700,521-111,700,536 , GRCh37.p13 chr11: 111,571,245-111,571,260 SIK2, PPP2R1B
    nsv5127167mobile element insertion1nstd203human GRCh38 chr11: 111,766,668-111,766,668 , GRCh37.p13 chr11: 111,637,392-111,637,392 , GRCh37.p13 chr11|NW_003871080.1: 18,660-18,660 PPP2R1B
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